Gene/Event |
Cancer Type |
Patient |
Variant |
Mutation Level |
CNTNAP2 |
Breast Cancer | p123_case8 |
p.S221C |
Trunk mutation |
CNTNAP2 |
Colorectal Cancer | p001_PCRC03 |
Chr7:147815318:C>A |
Trunk mutation |
CNTNAP2 |
Colorectal Cancer | p001_PCRC13 |
Chr7:148080940:G>A |
Private mutation |
CNTNAP2 |
Colorectal Cancer | p014_CRC2 |
p.R1284W |
Private mutation |
CNTNAP2 |
Colorectal Cancer | p034_MSU2 |
Chr7:147869436:T>C |
Trunk mutation |
CNTNAP2 |
Colorectal Cancer | p104_UC02 |
p.E582G |
Branch mutation |
CNTNAP2 |
Colorectal Cancer | p104_UC05 |
p.F89V |
Branch mutation |
CNTNAP2 |
Colorectal Cancer | p155_p493 |
p.L765L |
Private mutation |
CNTNAP2 |
Colorectal Cancer | p155_p497 |
p.Q514P |
Private mutation |
CNTNAP2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC007 |
p.Q792H |
Private mutation |
CNTNAP2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC007 |
p.S339G |
Private mutation |
CNTNAP2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC012 |
p.G388R |
Branch mutation |
CNTNAP2 |
Esophageal Squamous Cell Carcinoma | p124_ESCC035 |
p.G70fs |
Private mutation |
CNTNAP2 |
Esophageal Squamous Cell Carcinoma | p128_P15 |
Chr7:147183107:G>A |
Private mutation |
CNTNAP2 |
Esophageal Squamous Cell Carcinoma | p128_P21 |
Chr7:147183097:G>C |
Private mutation |
CNTNAP2 |
Esophageal Squamous Cell Carcinoma | p139_EC0988 |
p.G834X |
Private mutation |
CNTNAP2 |
Esophageal Squamous Cell Carcinoma | p139_EC1001 |
p.D880N |
Private mutation |
CNTNAP2 |
Gastric Adenocarcinoma | p011_MSS1 |
p.P153L |
Private mutation |
CNTNAP2 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.S570S |
Trunk mutation |
CNTNAP2 |
Gastric Adenocarcinoma | p011_MSI-H2 |
p.L1138L |
Private mutation |
CNTNAP2 |
Gastric Carcinoma | p106_GC02 |
p.G452G |
Private mutation |
CNTNAP2 |
Gastric Carcinoma | p106_GC08 |
p.K635T |
Trunk mutation |
CNTNAP2 |
Gastric Carcinoma | p106_GC09 |
p.L1152F |
Private mutation |
CNTNAP2 |
Gastric Carcinoma | p106_GC09 |
p.D1101D |
Private mutation |
CNTNAP2 |
Gastric Carcinoma | p106_GC09 |
p.E177D |
Private mutation |
CNTNAP2 |
Gastric Carcinoma | p106_GC15 |
p.A11V |
Private mutation |
CNTNAP2 |
Anaplastic Astrocytoma | p070_HGG1 |
Chr7:146536633:G>T |
Private mutation |
CNTNAP2 |
Glioblastoma | p113_case01 |
p.S586R |
Private mutation |
CNTNAP2 |
Glioblastoma | p113_case14 |
p.S586R |
Private mutation |
CNTNAP2 |
Glioblastoma | p113_case26 |
p.S586R |
Private mutation |
CNTNAP2 |
Glioma | p168_P01 |
p.A1239V |
Branch mutation |
CNTNAP2 |
Hepato-Cholangiocarcinoma | p078_p4 |
p.S820G |
Trunk mutation |
CNTNAP2 |
Intrahepatic Cholangiocarcinoma | p080_ICC1370 |
p.A470D |
Private mutation |
CNTNAP2 |
Hepatocellular Carcinoma | p061_P02 |
Chr7:146805344:C>A |
Private mutation |
CNTNAP2 |
Non-Small Cell Lung Cancer | p007_781 |
Chr7:147092727 |
Branch mutation |
CNTNAP2 |
Lung Adenocarcinoma | p017_330 |
Chr7:148106399:G>T |
Trunk mutation |
CNTNAP2 |
Lung Adenocarcinoma | p017_317ss |
Chr7:148143135:C>A |
Trunk mutation |
CNTNAP2 |
Large Cell Carcinoma | p100_p1 |
Chr7:146805443:G>C |
Branch mutation |
CNTNAP2 |
Non-Small Cell Lung Cancer | p107_P016 |
p.W833C |
Branch mutation |
CNTNAP2 |
Lung Adenocarcinoma | p134_A102 |
p.K954N |
Private mutation |
CNTNAP2 |
Lung Cancer | p154_p1 |
p.L426I |
Private mutation |
CNTNAP2 |
Melanoma | p043_F |
p.E37K |
Trunk mutation |
CNTNAP2 |
Melanoma | p043_F |
p.S687F |
Trunk mutation |
CNTNAP2 |
Ovarian Cancer | p144_AOCS093 |
p.G1207G |
Trunk mutation |
CNTNAP2 |
Pancreatic Cancer | p054_Pa04 |
- |
Trunk mutation |
CNTNAP2 |
Renal Cell Carcinoma | p073_RCC3 |
Chr7:147401440:C>T |
Private mutation |
CNTNAP2 |
Urothelial Carcinoma | p031_WCM077 |
p.Y681* |
Private mutation |
CNTNAP2 |
Urothelial Carcinoma | p031_WCM233 |
p.Y602* |
Private mutation |
CNTNAP2 |
Urothelial Carcinoma | p142_p07 |
- |
Private mutation |
CNTNAP2 |
Urothelial Carcinoma | p142_p36 |
- |
Private mutation |